CEPHALOSPORIN COMPOUNDS, THEIR PHARMACEUTICALLY ACCEPTABLE NONTOXIC SALTS, PHYSIOLOGICALLY HYDROLYZABLE ESTERS, ISOMERS HAVING E-CONFIGURATION OF DOUBLE BOND IN PROPENYL GROUP, SYN-ISOMERS AND OPTICAL ISOMERS AND A METHOD OF THEIR SYNTHESIS Russian patent published in 1997 - IPC

Abstract RU 2098420 C1

FIELD: organic chemistry, antibiotics. SUBSTANCE: product: cephalosporin of the general formula (I): , its pharmaceutically acceptable nontoxic salt, physiologically hydrolyzable ester, hydrate or solvate or its isomers where Q means CH or N; R1 means hydrogen or amino-protective group; R2 and R3 can be similar or different and mean independently hydrogen or hydroxy-protective group; or R2 and R3 together can form cyclic diol-protective group; R4 means hydrogen or carboxyl-protective group; R5,R6 and R7 independently mean hydrogen, amino or substituted amino, hydroxy, alkoxy, C1-4-alkyl, carboxyl or alkoxycarbonyl, or R5 and R6 together with carbon atoms to which they bound can form C3-C7-cycle. EFFECT: improved method of synthesis. 4 cl, 2 tbl

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RU 2 098 420 C1

Authors

Dzhae Khong Jeo[Kr]

Chan Sik Bang[Kr]

Dzhong Chan Lim[Kr]

Jung Min Vu[Kr]

Deog Kho Jang[Kr]

Se Kho Kim[Kr]

Dzhae Khun Dzheon[Kr]

Mu Jong Kim[Kr]

Sam Sik Kim[Kr]

Tae Khi Li[Kr]

Jong Tsu Kim[Kr]

Khun Seung Okh[Kr]

Dates

1997-12-10Published

1994-09-09Filed